Canonical Allele Identifier: PA2829599079
Gene: HADH HGNC NCBI

Linked Data

ClinVar Variation Id: 211127

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005318.6:p.Gln152His
CA209330
NM_005327.7:c.456G>T
CA357832852
NM_005327.7:c.456G>C